| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:13627360-13627550 | Rare:57 | ||||
| chr4:13627641-13627976 | Common:7; Rare:417 | ||||
| chr4:13627910-13628310 | Common:3; Rare:107 | ||||
| chr4:15001910-15002567 | Common:9; Rare:753 | ||||
| chr4:15002660-15003313 | Common:20; Rare:1244 | ||||
| chr4:15003245-15003645 | Common:8; Rare:155 | ||||
| chr4:15003632-15004426 | Common:12; Rare:519 | ||||
| chr4:15479268-15479740 | Common:4; Rare:182 | ||||
| chr4:15526730-15527250 | Common:3; Rare:139 | ||||
| chr4:15527425-15527552 | Rare:32; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:15655001-15655595 | Common:13; Rare:784 | ||||
| chr4:15659755-15660155 | Common:1; Rare:71 | ||||
| chr4:15681081-15681930 | Common:22; Rare:984 | ||||
| chr4:15682179-15682579 | Common:2; Rare:120 | ||||
| chr4:16225660-16226239 | Common:8; Rare:364 |